Variant #0000524236 (NC_000005.9:g.136993942T>C, NM_017415.2:c.781A>G (KLHL3))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.136993942T>C
DNA change (hg38) g.137658253T>C
Published as KLHL3(NM_001257194.1):c.685A>G (p.(Asn229Asp))
ISCN -
DB-ID KLHL3_000005
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPA0 NM_006805.3 -?/. - c.*94896A>G r.(=) p.(=)
KLHL3 NM_017415.2 -?/. - c.781A>G r.(?) p.(Asn261Asp)


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